Making available information from studies sponsored by the pharmaceutical industry: some current practices |
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Authors: | O'Kelly Michael Julious Steven A Pyke Stephen Day Simon Todd Sue Seldrup Jorgen Matcham James |
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Affiliation: | Quintiles Ireland Ltd, Dublin, Ireland. mokelly@quintiles.com |
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Abstract: | Since the web-based registry ClinicalTrials.gov was launched on 29 February 2000, the pharmaceutical industry has made available an increasing amount of information about the clinical trials that it sponsors. The process has been spurred on by a number of factors including a wish by the industry to provide greater transparency regarding clinical trial data; and has been both aided and complicated by the number of institutions that have a legitimate interest in guiding and defining what should be made available. This article reviews the history of this process of making information about clinical trials publicly available. It provides a reader's guide to the study registries and the databases of results; and looks at some indicators of consistency in the posting of study information. |
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Keywords: | disclosure clinical trials publication bias pharmaceutical industry regulatory requirements clinical trial registry |
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